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- explain part A by first drawing all the resonance structures for the four compounds please. and then write the explanaiton. HANDDRAW it instead of using text. thanksi need help please like asapDraw the major organic product for each of the hydroboration‑oxidation reactions. Disregard stereochemistry.
- Predict the pathway (SN1/SN2) and structure of the major product in the following reaction HBr o.,Q4: Rank the relative nucleophilicity of halide ions in water solution and DMF solution, respectively. F CI Br | Q5: Determine which of the substrates will and will not react with NaSCH3 in an SN2 reaction to have a reasonable yield of product. NH2 Br Br Br OH Br1. Predict the major organic product(s) for each of the following reactions. Be sure to clearly indicate the proper stereochemical relationships between groups (if appropriate), and write the word "racemic" next to any compound that is formed as a racemic mixture. a. b. C. d. H H3C CH3 aq. KOH, A H₂N CH3 OH CH3 HO Ph H CH3OH PhH, A + Ph 'N' H CH3 HS SH BF3 teYr + {,,trs,£ CH3 H3C H e. HO N H2SO4 Ph. CH3 f. CH3 p-TSOH H3C H 2 eq. CH3OH g. h. H3C Ph H3O+ Ph H HO-NH2 AcOH
- The last step in the synthesis of a series of potential anti- inflammatory agents is shown below (Ar is some arene ring. The reaction results in the loss of the elements of water (that is, the product has two less H's and one less O than the reagent shown). Give the structure of the product and the full, step-by-step mechanism for its formation. Ar Ar Cat. Na ome Me of11) Which of the following is (2R, 3S)-2,3-pentanediol? Он Он он он он OH он он A D Ol.. B.Draw the organic products formed in each reaction.